chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
138560203285602033GA16GENIChomozygous126070434
138560207185602072CT14GENIChomozygous126070435
138560211085602111TC14GENIChomozygous118464993
138560229485602295GA35GENIChomozygous118464994
138560229785602298CA35GENIChomozygous114422428
138560317785603178TC49GENIChomozygous114422430
138560380485603805AT46GENIChomozygous114422432
138560395085603957CTGGGTG44GENIChomozygous129082597
138560263485602635AG25GENIChomozygous118502587
138560264785602647TA25GENIChomozygous129082593
138560269785602701ATAC26GENIChomozygous129082594
138560272385602723AC32GENIChomozygous129082595
138560276385602763ATAT31GENIChomozygous129082596
138560271085602711TC32GENIChomozygous114645908
138560463985604640TC46GENIChomozygous114422434
138560539685605397AG48GENIChomozygous114422436
138560624885606249TC46GENIChomozygous114422438
138560697185606971TATT47GENIChomozygous129082598
138560722785607228CT50GENIChomozygous114422440
138560777185607772GC27GENIChomozygous114422442
138560785685607857CA36GENIChomozygous114422444
138560961385609614GA49GENIChomozygous114422446
138561008485610085TA28GENIChomozygous114422452
138561010185610102CG33GENIChomozygous114422454
138561012685610127CT36GENIChomozygous114422456
138561013585610136CA42GENIChomozygous114422458
138561108985611090GA45GENIChomozygous114422460
138561222185612222TC53GENIChomozygous114422462
138561326685613272GGTCTT55GENIChomozygous129082599
138561335985613360TG56GENIChomozygous114422464
138561358885613589CG60GENIChomozygous114422466
138561513385615134GA35GENIChomozygous114422470
138561524685615251GGGAT41GENIChomozygous129082600
138561568785615688AG55GENIChomozygous114422472
138561572285615723AG45GENIChomozygous114422474
138561553685615537CG14GENICpossibly homozygous114830687
138561823185618232CT45GENIChomozygous114422476